IdentityE High Definition Proteomics系统定义了严密的蛋白质识别的新标准体系。专门设计用于权威和全面的定性分析，沃特世解决方案使得蛋白质组学研究人员可参照色谱滞留时间、前体和产物离子块、结构意义、生物环境以及对多种肽段的识别，自信地识别蛋白质。
The IdentityE High Definition Proteomics System combines UPLC/MSE data with a comprehensive peptide ion accounting informatics solution to catalog complex protein digest mixtures.
The system features:
The IdentityE system dramatically increases sequence coverage in this study of a digested cytosolic fraction from an E.coli lysate (three technical replicas).
Data Acquisition by Alternating Spectra Energy
UPLC/MSE is a unique, patented technology that has an extremely high duty cycle, allowing the acquisition of high quality accurate mass data in a simple, unbiased manner.
UPLC/MSE acquires data with two rapidly alternating MS functions. The first contains exclusively low-energy mass spectra, the second is composed of mass spectra acquired at elevated collision energy (designated as MSE). The resulting data set contains a comprehensive time-resolved record of all detectible precursor and product ions.
Precursor and product ions are associated by both retention time alignment and peak shape, enabling even chimeric peptides and overlapping ion clusters to be successfully handled. The resulting time-aligned precursor and product ion mass lists are used for peptide identification with the IdentityE System’s peptide ion informatics.
Peptide Ion Informatics
This bioinformatics software visualizes peptides and proteins with a new multi-layered physicochemical model of protein primary structure. Peptide ion accounting informatics adapts to each new UPLC/MSE data set using a pre-assessment survey. 250 identified peptides, per run, are used to fine-tune many of the 14 models used for both peptide and protein authentication.
After pre-assessment, an iterative database search strategy is initiated, identifying the most abundant protein within a sample by matching peptides, modified peptides, and retention times. An estimate of the absolute concentration of each protein is made by reference to an internal (protein) standard, allowing the fractions of all theoretical tryptic peptides that are plausibly detectable to be predicted. Proteins identified with fewer than the predicted number of peptides are sequence mapped for evidence of C/N-terminal processing.
When the most abundant protein is conclusively identified, all assigned peptide ions are subtracted from the working image of the data.
Multi-layered Physicochemical Model
The IdentityE System features Waters peptide ion accounting informatics. This technology visualizes peptides and proteins with a multi-layered physicochemical model of protein primary structure, developed from a post-genomic understanding of protein characteristics – an advantage unavailable in any other protein identification tool and unique to the IdentityE system.
Peptide ion accounting informatics adapts to each new UPLC/MSE data set utilizing a pre-assessment survey. 250 unambiguously identified (abundant) peptides, per run, are used to fine-tune many of the 14 models used for both peptide and protein authentication. Automatic adjustment of these models on an injection-by-injection basis provides the means for the software to handle changes in chromatographic conditions (buffers and columns), enzymatic specificity, and sample complexity.
Fourteen different physicochemical attributes are automatically considered to maximize peptide identification confidence. Other conventional protein identification systems utilize only a small number of these characteristics.
Iterative Protein Identification
When the most abundant protein is conclusively identified, all assigned peptide ions are subtracted from the working image of the data. The process is then repeated for the next most abundant protein, as many times as is necessary to account for as many ions as possible within the UPLC/MSE data set. As more proteins are identified, and their associated peptide ions are removed, the working image of the data becomes less complex – revealing proteins of decreasing abundance for identification.
Utilizing the 14 physicochemical models of the peptide ion accounting informatics, proteins are identified in order of their abundance, thus increasing the selectivity, specificity, and sensitivity of each iterative protein identification. The above data illustrates that proteins are being identified and their respective ions depleted by their abundance.
More Peptides per Protein
The IdentityE System identifies more peptides per protein, providing both higher sequence coverage and rigor to the protein ID. Over 95% (389) of the proteins were identified with greater than three peptides to match, compared to the LTQ Orbitrap and the LTQ with only 65% (244) and 33% (88), respectively.